openFDA Device API
Device-domain endpoints covering MAUDE adverse event reports, device classification, 510(k) premarket notifications, PMA premarket approvals, UDI Unique Device Identifier records, device recall enforcement reports, device recalls, registration and listing, and the COVID-19 in vitro diagnostic serology test results dataset.
Documentation
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https://open.fda.gov/apis/device/
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https://open.fda.gov/apis/device/event/
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https://open.fda.gov/apis/device/classification/
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https://open.fda.gov/apis/device/enforcement/
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https://open.fda.gov/apis/device/recall/
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https://open.fda.gov/apis/device/510k/
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https://open.fda.gov/apis/device/pma/
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https://open.fda.gov/apis/device/udi/
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https://open.fda.gov/apis/device/registrationlisting/
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https://open.fda.gov/apis/device/covid19serology/